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FDA 510(k)

THERASNORE

K-Number: K926382 · 1993-07-08

ApplicantDr. Thomas E. Meade
Decision Date1993-07-08
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THERASNORE is the device name listed in this FDA 510(k) record. The listed applicant is Dr. Thomas E. Meade. It received FDA 510(k) clearance on 1993-07-08 under 510(k) number K926382. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERASNORE?

THERASNORE is a medical device that received FDA 510(k) clearance on 1993-07-08. The listed applicant is Dr. Thomas E. Meade. The 510(k) number is K926382.

When did THERASNORE receive FDA 510(k) clearance?

THERASNORE received FDA 510(k) clearance on 1993-07-08, under 510(k) number K926382.

Who is the listed applicant for THERASNORE?

The FDA 510(k) record lists Dr. Thomas E. Meade as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THERASNORE?

The FDA product code for THERASNORE is LRK.

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Related Devices (Code: LRK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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